Canonical Allele Identifier: PA2829999381
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445386
ClinVar RCV Id: RCV003154796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala154Val
CA379965013
NM_024424.5:c.461C>T